TiCl4 induced anti-Markovnikov rearrangement

Stereoisomeric bicyclic tert-alcohols afforded identical ring-expansion products via cationic anti-Markovnikov rearrangement from perpendicular tert-cations into identical six-membered ring secondary cations by the treatment with TiCl4. These results provide evidence that the reaction takes place by the cationic stepwise mechanism. [reaction: see text]     

Design and synthesis of 5'-deoxy-5'-phenyladenophostin A, a highly potent IP3 receptor ligand

[structure: see text] 5'-Deoxy-5'-phenyladenophostin A (5), designed as a useful IP(3) receptor ligand based on the previous structure-activity relationship studies, was successfully synthesized via two key stereoselective glycosidation steps. This compound proved to be a highly potent IP(3) receptor agonist.     

Current-driven resonant excitation of magnetic vortices

A magnetic vortex core in a ferromagnetic circular nanodot has a resonance frequency originating from the confinement of the vortex core. By the micromagnetic simulation including the spin-transfer torque, we show that the vortex core can be resonantly excited by an ac (spin-polarized) current through the dot and that the resonance frequency can be tuned by the dot shape. The resistance measurement under the ac current successfully detects the resonance at the frequency consistent with the simulation.     

On a generalization of distance sets

A subset X in the d-dimensional Euclidean space is called a k-distance set if there are exactly k distinct distances between two distinct points in X and a subset X is called a locally k-distance set if for any point x in X, there are at most k distinct distances between x and other points in X.Delsarte, Goethals, and Seidel gave the Fisher type upper bound for the cardinalities of k-distance sets on a sphere in 1977. In the same way, we are able to give the same bound for locally k-distance sets on a sphere. In the first part of this paper, we prove that if X is a locally k-distance set attaining the Fisher type upper bound, then determining a weight function w, (X,w) is a tight weighted spherical 2k-design. This result implies that locally k-distance sets attaining the Fisher type upper bound are k-distance sets. In the second part, we give a new absolute bound for the cardinalities of k-distance sets on a sphere. This upper bound is useful for k-distance sets for which the linear programming bound is not applicable. In the third part, we discuss about locally two-distance sets in Euclidean spaces. We give an upper bound for the cardinalities of locally two-distance sets in Euclidean spaces. Moreover, we prove that the existence of a spherical two-distance set in (d−1)-space which attains the Fisher type upper bound is equivalent to the existence of a locally two-distance set but not a two-distance set in d-space with more than d(d+1)/2 points. We also classify optimal (largest possible) locally two-distance sets for dimensions less than eight. In addition, we determine the maximum cardinalities of locally two-distance sets on a sphere for dimensions less than forty.     

Metric packing for K 3+K 3

In this paper, we consider the metric packing problem for the commodity graph of disjoint two triangles K ₃+K ₃, which is dual to the multiflow feasibility problem for the commodity graph K ₃+K ₃. We prove a strengthening of Karzanov’s conjecture concerning quarterintegral packings by certain bipartite metrics.     

Glass-forming Photoconductive Organic Compounds II1: Glass-forming Properties of 1,3,5-Triaryl-2-pyrazolines

Glass-forming properties of 2-pyrazoline derivatives were examined and discussed in terms of the molecular structure. The results show that the molecular shape of 1,3,5-triaryl-2-pyrazolines is responsible for the glass-forming properties of these compounds. Glass transition points of several 1,3,5-triaryl-2-pyrazoline derivatives were measured.     

Hydrogen Intercalation in Potassium-C60

Abstract

Solid state ¹H NMR of (KH)₃C₆₀ was measured in the temperature range between ?80 and 60 °C. A doublet spectrum composed of main peak at ?7.0 ppm and shoulder peak at ～0 ppm was observed at room temperature. The negative chemical shift of the main peak indicates that hydrogen in (KH)₃C₆₀ exists as a hydride-like ion. The 60 °C spectrum became singlet at ?5.8 ppm due to motional narrowing.     

EXAFS and XANES Studies on 3d Transition Metal Intercalation Compounds M x TiS2

Abstract

EXAFS and XANES spectra of Ti K-edge have been measured for 3d transition metal intercalation compounds M _x TiS₂ (M = Mn, Fe, Co and Ni; x ≤ 0.33). We have found that the interatomic distance between Ti and the first nearest neighbor S atoms, R(Ti-S), increases with the guest concentration x. The variation in XANES spectra with x reveals the reduction of the valence state of Ti atoms upon intercalation of M. From these results as well as the M K-edge EXAFS data studied previously, we have proposed a simple model on the local structure of M _x TiS₂ to reproduce the observed values of R(Ti-S) by averaging local shift of S atoms caused by intercalation.     

Effects of pressure and temperature on the solubility of monosodium L-glutamate monohydrate in water

Abstract

The solubility of monosodium L-glutamate monohydrate (MSG.H₂O) in water was measured at pressures in the range of 0.10-300MPa and 298.15K. The density of MSG solution at high concentrations and heat of solution at saturated concentration were also measured at atmospheric pressure. The solubility, m_s, increased with increasing pressure and the pressure coefficient, Θ_p, [?(? In m_s,? p)_T] at 0.10 MPa was (2.0 ± 0.1) × 10-¹⁰Pa-1. It agrees well with (2.1 ±0.2)× 10-¹⁰ Pa-¹ thermodynamically estimated using the partial molar volume, the activity coefficient of the solute in solution, and the molar volume of the crystal. The excellent agreement at 0.10MPa gives us confidence in the solubility data at higher pressures. The heat of solution data and other pertinent values were used to calculate the temperature coefficient of solubility, Θ_T [? (? In m_s/?(1/T))_p], by a thermodynamic equality. The resulting Θ_T compares well with the data directly measured by Ogawa.